MedPath

Pressure Ulcer Prevention: Turning for Ulcer Reduction

Phase 3
Completed
Conditions
Pressure Ulcers
Interventions
Procedure: Turning or repositioning schedule
Registration Number
NCT00665535
Lead Sponsor
The University of Texas Health Science Center, Houston
Brief Summary

The purpose of the study is to determine the optimal frequency of repositioning nursing facility residents with limited mobility who are cared for on a high density foam mattress in order to prevent bed sores. It is hypothesized that participants at moderate risk (Braden Scale Scores 13-14) who are turned every 3 or 4 hours and participants at high risk (Braden Scores 10-12) turned every 3 or 4 hours will not have a higher incidence of ulcers than those residents turned every 2 hours.

Detailed Description

The purpose of this multi-site, randomized, controlled trial is to determine the optimal frequency of repositioning nursing facility residents with mobility limitations who are at moderate and high risk for pressure ulcer development who are cared for on high density foam mattresses for the purpose of preventing pressure ulcers. Pressure ulcers result primarily from pressure over a bony prominence that occludes blood flow to tissues. Traditionally, soft surfaces over mattress and repositioning individuals every 2 hours to relieve pressure have been the gold standard of care to prevent ulcers. Recent improvements in support surfaces may reduce the need for 2-hour repositioning. The specific aims of this study are to determine if: 1) there is a significant difference in the incidence of pressure ulcers among: a) moderate risk (Braden Scale Score, 13-14) residents randomly assigned to be repositioned every 2-, compared with every 3- or 4- hours; or b) high risk (Braden Scale Score, 10-12) residents who are turned every 2- compared with every 3- or 4-hours; 2) mobility (spontaneous or assisted) measured by actigraphy is a significant covariate with repositioning frequency in the incidence of pressure ulcers and 3) resident characteristics and resident influencing factors are significant covariates of repositioning schedules on pressure ulcer incidence. A 2 X 2/2 X 3 experimental design is used in which participants at two levels of risk (moderate or high) for pressure ulcer development are randomly assigned to one of 3 repositioning schedules every 2-hours (the current standard of care), contrasted with 3- or 4- hours carried out for 3 weeks. Actigraphs worn for 7 days (Tuesday to Tuesday) will determine if mobility is a significant covariate. Residents (1080) who are over 65 years, able to give consent or have a surrogate who can give consent and are at moderate or high risk for pressure ulcers will be invited to participate. Nursing facilities are selected because of their ability to follow a research protocol and submit data according to protocol requirements, and who have a reputation for good care are being selected for participation. Participants will be randomly assigned to a repositioning schedule that will be carried out by a Certified Nursing Assistants (CNA) who will document time of each repositioning. A CNA supervisor monitors repositioning and documentation frequently. Data are FAXED to and monitored by the investigators daily. With the exception of the repositioning intervention, participants will receive the same preventive care as all residents. The primary outcome of this study, pressure ulcers (yes/no) will be documented by a nurse assessor who will be masked to the repositioning timing. Data analysis and management will be performed by ISIS. The goal of this study is to shape Nursing Facility policy by defining how level of risk, mobility, and frequency of repositioning of residents can reduce the incidence of pressure ulcers and improve resident outcomes. Less frequent repositioning would allow residents longer periods of sleep, would reduce staff time for repositioning, and allow more efficient allocation of time.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
967
Inclusion Criteria

Participants will:

  • Be free of pressure ulcers upon admission to the study.
  • Have a Braden Scale Score between 10 - 12 (high risk) or 13 -14 (moderate risk) within one week of admission (new residents) or greater than 90 days (established residents) of study participation
  • Have a high-density foam replacement mattress in use or can be transferred to such a mattress.
  • Are 65 years or older. Younger residents are present in fewer numbers and may have different health issues and co-morbidities than older residents.
  • Can legally grant consent to participate or have available surrogates to grant consent. If able, participant should assent when a surrogate grants consent.
  • Expected to have a length of stay of 21 days or greater.
Exclusion Criteria
  • Pressure ulcer is present upon initial examination.
  • The Braden Scale score is 15 or greater indicating mild risk or no risk, or 9 or below indicating very high risk.
  • The resident cannot be turned on 3 anatomical surfaces (side, back, side) or has a contraindication to repositioning.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
2. High RiskTurning or repositioning scheduleHigh risk for pressure ulcers according to the Braden Scale for Predicting Pressure Sore Risk (Score 10-12)
1. Moderate RiskTurning or repositioning scheduleModerate risk for pressure ulcers according to the Braden Scale for Predicting Pressure Sore Risk (Score 13 and 14)
Primary Outcome Measures
NameTimeMethod
Pressure ulcers, present (stage)or absentEnd of 3rd week or conclusion of participation
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (26)

Fairmount at aBreckenridge Village

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Willoughby, Ohio, United States

Yee Hong Scarborough

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Scarborough, Ontario, Canada

Glencroft Care Center

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Glendale, Arizona, United States

Linda Valley Nursing Facility

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Loma Linda, California, United States

Miami Jewish Home & Hospital

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Miami, Florida, United States

Garden Crest Convalescent Hospital

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Los Angeles, California, United States

St. Catherine Laboure Manor

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Jacksonville, Florida, United States

Kindred Bremen Health Care Center

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Bremen, Indiana, United States

Palatka Health Care Center

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Palatka, Florida, United States

Monroe Community Hospital

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Rochester, New York, United States

Gurwin Jewish Nursing and Rehabilitation Center

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Commack, New York, United States

Tower Hill Center for Health and Rehabilitation

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Canton, Massachusetts, United States

BlumenthalJewish Nursing and Rehabilitation

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Greensboro, North Carolina, United States

Dorothy Love Retirement Community

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Sidney, Ohio, United States

Hennis Care Center

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Dover, Ohio, United States

Park Vista Retirement Community

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Youngstown, Ohio, United States

Kindred Fairpark Health Care Center

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Maryville, Tennessee, United States

Kindred Loudon Healthcare Center

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Loudon, Tennessee, United States

Specialty Care of Mississauga Road

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Mississauga, Ontario, Canada

Signature HealthCare of Columbia

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Columbia, Tennessee, United States

Tyndall Nursing Home

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East Missassauga, Ontario, Canada

Malton Village Long Term Care Center

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Mississauga, Ontario, Canada

Asbury Place Maryville

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Maryville, Tennessee, United States

Leisure World Lawrence

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Toronto, Ontario, Canada

Shepherd Lodge

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Scarborough, Ontario, Canada

Villa Leonardo Gambin Specialty Care

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Woodbridge, Ontario, Canada

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